Fig. 3.
Fig. 3. Etoposide (50 μmol/L), Ara-C (100 μmol/L), and doxorubicin (50 μmol/L) induced apoptosis of HL-60/neo, U937, and Jurkat cells. / Cells were treated with the drugs at the indicated concentrations for 6 hours followed by incubation for 18 hours in drug-free medium. After these treatments, the percentage of apoptotic cells was determined by Annexin V staining followed by flow cytometry (A). Molecular events of apoptosis induced by etoposide, Ara-C, or doxorubicin (B). Cells were treated with the indicated drugs for 6 hours, and then cell lysates were obtained for Western analyses of procaspase-3, procaspase-9, cytosolic cyt c, and Bid protein. Alternatively, Western analysis of XIAP and survivin was performed on the cell lysates (C) (see “Results”).

Etoposide (50 μmol/L), Ara-C (100 μmol/L), and doxorubicin (50 μmol/L) induced apoptosis of HL-60/neo, U937, and Jurkat cells.

Cells were treated with the drugs at the indicated concentrations for 6 hours followed by incubation for 18 hours in drug-free medium. After these treatments, the percentage of apoptotic cells was determined by Annexin V staining followed by flow cytometry (A). Molecular events of apoptosis induced by etoposide, Ara-C, or doxorubicin (B). Cells were treated with the indicated drugs for 6 hours, and then cell lysates were obtained for Western analyses of procaspase-3, procaspase-9, cytosolic cyt c, and Bid protein. Alternatively, Western analysis of XIAP and survivin was performed on the cell lysates (C) (see “Results”).

Close Modal

or Create an Account

Close Modal
Close Modal